We have taken all reasonable efforts to ensure that the results produced by SNPCheck are accurate and reliable. All variant data and associated annotations are reproduced from NCBI dbSNP, 1000 Genomes Project and the Exome Sequencing Project and may not always be correct. NGRL Manchester (Central Manchester University Hospitals NHS Foundation Trust) is not responsible for the content of dbSNP, 1000 Genomes Project and Exome Sequencing Project datasets and makes no judgements or computations about the validity of variant data or potential effects on the diagnostic process which SNPCheck presents. SNPCheck is a tool to simplify the process of checking primers for the presence of known SNPs, but users must use due diligence to ensure the validity of these results. We make no warranty, express or implied, as to SNPCheck's accuracy nor that the information is fit for a particular purpose, and will not be held responsible for any consequences arising out of any inaccuracies or omissions. Individuals, organisations and companies who use SNPCheck do so on the understanding that no liability whatsoever either direct or indirect shall rest upon NGRL Manchester (Central Manchester University Hospitals NHS Foundation Trust) or any of their employees or agents for the effects of any product, process or method that may be produced or adopted by any part, notwithstanding that the formulation of such product, process or method may be based upon information here provided.